SYNTHESIS AND INVITRO ACTIVITY OF THE PENEM ANTIBIOTICS

[1] NEW SYNTHESIS OF PENEMS, THE OXALIMIDE CYCLIZATION REACTION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (22) : 6138 - 6139

[2] AFONSO A, 1985, SPEC PUBL ROYAL SOC, V52, P266

[3] AIMETTI JA, 1979, TETRAHEDRON LETT, P3805

[4] STRUCTURE AND ABSOLUTE-CONFIGURATION OF THIENAMYCIN [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1978, 100 (20) : 6491 - 6499

[5] DESULFURATIVE APPROACHES TO PENEM ANTIBIOTICS .6. FROM PENAM METHYL-ESTERS TO PENEM ACETONYL ESTERS - A FULLY CONSERVATIVE CONVERSION [J]. TETRAHEDRON LETTERS, 1984, 25 (37) : 4171 - 4174

[6] SILVER-ASSISTED 1,2-CLEAVAGE OF PENICILLINS - A 3-STEP SYNTHESIS OF OPTICALLY-ACTIVE PENEMS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (22) : 6398 - 6399

[7] ALPEGIANI M, 1981, GAZZ CHIM ITAL, V114, P391

[8] A NEW ROUTE TO PENEMS AND CARBAPENEMS [J]. TETRAHEDRON LETTERS, 1984, 25 (22) : 2395 - 2398

[9] STEREOSELECTIVITY IN 6-HALOPENICILLANATE GRIGNARD REACTIONS [J]. TETRAHEDRON LETTERS, 1986, 27 (14) : 1545 - 1548

[10] 4,7-LACTAMS, INTERMEDIATES FOR PENEMS SYNTHESIS .2. TOTAL SYNTHESIS OF (+)-2,2-DIMETHYL-9-OXO-3-OXA-6-THIA-1-AZABICYCLO [5.2.01,7]NONANE [J]. TETRAHEDRON LETTERS, 1981, 22 (41) : 4145 - 4148

[1] NEW SYNTHESIS OF PENEMS, THE OXALIMIDE CYCLIZATION REACTION [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1982, 104 (22) : 6138 - 6139

[2] AFONSO A, 1985, SPEC PUBL ROYAL SOC, V52, P266

[3] AIMETTI JA, 1979, TETRAHEDRON LETT, P3805

[4] STRUCTURE AND ABSOLUTE-CONFIGURATION OF THIENAMYCIN [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1978, 100 (20) : 6491 - 6499

[5] DESULFURATIVE APPROACHES TO PENEM ANTIBIOTICS .6. FROM PENAM METHYL-ESTERS TO PENEM ACETONYL ESTERS - A FULLY CONSERVATIVE CONVERSION [J]. TETRAHEDRON LETTERS, 1984, 25 (37) : 4171 - 4174

[6] SILVER-ASSISTED 1,2-CLEAVAGE OF PENICILLINS - A 3-STEP SYNTHESIS OF OPTICALLY-ACTIVE PENEMS [J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1985, 107 (22) : 6398 - 6399

[7] ALPEGIANI M, 1981, GAZZ CHIM ITAL, V114, P391

[8] A NEW ROUTE TO PENEMS AND CARBAPENEMS [J]. TETRAHEDRON LETTERS, 1984, 25 (22) : 2395 - 2398

[9] STEREOSELECTIVITY IN 6-HALOPENICILLANATE GRIGNARD REACTIONS [J]. TETRAHEDRON LETTERS, 1986, 27 (14) : 1545 - 1548

[10] 4,7-LACTAMS, INTERMEDIATES FOR PENEMS SYNTHESIS .2. TOTAL SYNTHESIS OF (+)-2,2-DIMETHYL-9-OXO-3-OXA-6-THIA-1-AZABICYCLO [5.2.01,7]NONANE [J]. TETRAHEDRON LETTERS, 1981, 22 (41) : 4145 - 4148